This is a prospective, randomized, double-blind, sham treatment controlled multicenter study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
52
conduct treatment twice a week for 3 weeks and once a week for 4 weeks, total 10 times
Unnamed facility
Prague, Czechia
Unnamed facility
Hanover, Germany
Unnamed facility
Rostock, Germany
Tel Aviv Sourasky Medical Center
Tel Aviv, Israel
Clinical response
Time frame: at 8th week
Remission, Mayo scores, Mucosal healing, CRP
Time frame: at 8th and 16th week
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Unnamed facility
Hyōgo, Japan
Unnamed facility
Tokyo, Japan
Unnamed facility
Gothenburg, Sweden
Unnamed facility
Stockholm, Sweden
Unnamed facility
Oxford, United Kingdom
Unnamed facility
Southampton, United Kingdom